转移性结直肠癌患者的持续治疗和生存:真实世界前瞻性、纵向队列PROMETCO研究的结果

M. Koopman , R. Garcia-Carbonero , C. Pinto , A. Mitroshkin , G. Bodoky , L. Mineur , V. Bourgeois , M. Mare , A. Ruiz-Casado , A. Fernandez Montes , J.M. O’Connor , A. Sullivan , E. Choucair , B. Chevallier , F. Marti Marti , J.-B. Bachet
{"title":"转移性结直肠癌患者的持续治疗和生存:真实世界前瞻性、纵向队列PROMETCO研究的结果","authors":"M. Koopman ,&nbsp;R. Garcia-Carbonero ,&nbsp;C. Pinto ,&nbsp;A. Mitroshkin ,&nbsp;G. Bodoky ,&nbsp;L. Mineur ,&nbsp;V. Bourgeois ,&nbsp;M. Mare ,&nbsp;A. Ruiz-Casado ,&nbsp;A. Fernandez Montes ,&nbsp;J.M. O’Connor ,&nbsp;A. Sullivan ,&nbsp;E. Choucair ,&nbsp;B. Chevallier ,&nbsp;F. Marti Marti ,&nbsp;J.-B. Bachet","doi":"10.1016/j.esmogo.2025.100214","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>PROMETCO is the first international, prospective study investigating the continuum of care, including prescribing patterns, efficacy and safety in patients with metastatic colorectal cancer (mCRC) at later therapy lines in a real-world setting.</div></div><div><h3>Materials and methods</h3><div>Adults with mCRC and two disease progressions since diagnosis of mCRC who were willing to receive subsequent treatment and gave informed consent were included. The study consisted of retrospective medical chart data collection pre-inclusion and a prospective observational period post-inclusion. Endpoint data presented include patient characteristics, treatment patterns and efficacy including progression-free survival (PFS) per treatment line and overall survival (OS).</div></div><div><h3>Results</h3><div>As of July 2023, 738 mCRC patients from 96 centres in 18 countries were recruited. 48.9% of patients had <em>RAS</em>-mutated and 5.0% <em>BRAF</em>-mutated mCRC. Between mCRC diagnosis and death or withdrawal, patients were frequently exposed to fluoropyrimidine (99.0%), irinotecan (96.2%), oxaliplatin (88.4%), anti-vascular endothelial growth factor (78.7%) and anti-epidermal growth factor receptor (40.1%). Median OS was 36.4, 7.1, and 6.6 months from mCRC diagnosis, inclusion into PROMETCO and third-line (3L) treatment initiation, respectively. Median PFS decreased significantly from first-line (9.2 months) to 3L (2.7 months) and remained consistent from 3L to sixth-line treatment (∼2.3 months). Median OS from diagnosis was 32.7, 26.8, and 40.6 months in <em>RAS</em>-mutated, <em>BRAF</em>-mutated, and <em>RAS/BRAF</em> wildtype mCRC patients, respectively.</div></div><div><h3>Conclusions</h3><div>PROMETCO provided information on real-world prescribing patterns and efficacy. OS from mCRC diagnosis and PFS from 3L and beyond were similar to previous long-term follow-up data from clinical trials.</div></div>","PeriodicalId":100490,"journal":{"name":"ESMO Gastrointestinal Oncology","volume":"9 ","pages":"Article 100214"},"PeriodicalIF":0.0000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Continuum of care and survival in patients with metastatic colorectal cancer: results of the real-world prospective, longitudinal cohort PROMETCO study\",\"authors\":\"M. Koopman ,&nbsp;R. Garcia-Carbonero ,&nbsp;C. Pinto ,&nbsp;A. Mitroshkin ,&nbsp;G. Bodoky ,&nbsp;L. Mineur ,&nbsp;V. Bourgeois ,&nbsp;M. Mare ,&nbsp;A. Ruiz-Casado ,&nbsp;A. Fernandez Montes ,&nbsp;J.M. O’Connor ,&nbsp;A. Sullivan ,&nbsp;E. Choucair ,&nbsp;B. Chevallier ,&nbsp;F. Marti Marti ,&nbsp;J.-B. Bachet\",\"doi\":\"10.1016/j.esmogo.2025.100214\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><div>PROMETCO is the first international, prospective study investigating the continuum of care, including prescribing patterns, efficacy and safety in patients with metastatic colorectal cancer (mCRC) at later therapy lines in a real-world setting.</div></div><div><h3>Materials and methods</h3><div>Adults with mCRC and two disease progressions since diagnosis of mCRC who were willing to receive subsequent treatment and gave informed consent were included. The study consisted of retrospective medical chart data collection pre-inclusion and a prospective observational period post-inclusion. Endpoint data presented include patient characteristics, treatment patterns and efficacy including progression-free survival (PFS) per treatment line and overall survival (OS).</div></div><div><h3>Results</h3><div>As of July 2023, 738 mCRC patients from 96 centres in 18 countries were recruited. 48.9% of patients had <em>RAS</em>-mutated and 5.0% <em>BRAF</em>-mutated mCRC. Between mCRC diagnosis and death or withdrawal, patients were frequently exposed to fluoropyrimidine (99.0%), irinotecan (96.2%), oxaliplatin (88.4%), anti-vascular endothelial growth factor (78.7%) and anti-epidermal growth factor receptor (40.1%). Median OS was 36.4, 7.1, and 6.6 months from mCRC diagnosis, inclusion into PROMETCO and third-line (3L) treatment initiation, respectively. Median PFS decreased significantly from first-line (9.2 months) to 3L (2.7 months) and remained consistent from 3L to sixth-line treatment (∼2.3 months). Median OS from diagnosis was 32.7, 26.8, and 40.6 months in <em>RAS</em>-mutated, <em>BRAF</em>-mutated, and <em>RAS/BRAF</em> wildtype mCRC patients, respectively.</div></div><div><h3>Conclusions</h3><div>PROMETCO provided information on real-world prescribing patterns and efficacy. OS from mCRC diagnosis and PFS from 3L and beyond were similar to previous long-term follow-up data from clinical trials.</div></div>\",\"PeriodicalId\":100490,\"journal\":{\"name\":\"ESMO Gastrointestinal Oncology\",\"volume\":\"9 \",\"pages\":\"Article 100214\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ESMO Gastrointestinal Oncology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2949819825000834\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ESMO Gastrointestinal Oncology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2949819825000834","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

prometco是第一个国际前瞻性研究,旨在调查转移性结直肠癌(mCRC)患者在现实世界中接受后期治疗的连续性治疗,包括处方模式、疗效和安全性。材料和方法纳入了自诊断为mCRC并有两种疾病进展的成年人,他们愿意接受后续治疗并给予知情同意。该研究包括纳入前的回顾性医学图表数据收集和纳入后的前瞻性观察期。终点数据包括患者特征、治疗模式和疗效,包括每条治疗线的无进展生存期(PFS)和总生存期(OS)。截至2023年7月,从18个国家的96个中心招募了738名mCRC患者。48.9%的患者发生ras突变,5.0%的患者发生braf突变。在mCRC诊断至死亡或停药期间,患者经常暴露于氟嘧啶(99.0%)、伊立替康(96.2%)、奥沙利铂(88.4%)、抗血管内皮生长因子(78.7%)和抗表皮生长因子受体(40.1%)。从mCRC诊断、纳入PROMETCO和三线(3L)治疗开始算起,中位OS分别为36.4、7.1和6.6个月。中位PFS从一线(9.2个月)显著下降到3L(2.7个月),从3L到六线治疗(~ 2.3个月)保持一致。RAS突变、BRAF突变和RAS/BRAF野生型mCRC患者自诊断起的中位生存期分别为32.7、26.8和40.6个月。结论prometco提供了真实世界的处方模式和疗效信息。mCRC诊断的OS和3L及以上的PFS与先前临床试验的长期随访数据相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Continuum of care and survival in patients with metastatic colorectal cancer: results of the real-world prospective, longitudinal cohort PROMETCO study

Background

PROMETCO is the first international, prospective study investigating the continuum of care, including prescribing patterns, efficacy and safety in patients with metastatic colorectal cancer (mCRC) at later therapy lines in a real-world setting.

Materials and methods

Adults with mCRC and two disease progressions since diagnosis of mCRC who were willing to receive subsequent treatment and gave informed consent were included. The study consisted of retrospective medical chart data collection pre-inclusion and a prospective observational period post-inclusion. Endpoint data presented include patient characteristics, treatment patterns and efficacy including progression-free survival (PFS) per treatment line and overall survival (OS).

Results

As of July 2023, 738 mCRC patients from 96 centres in 18 countries were recruited. 48.9% of patients had RAS-mutated and 5.0% BRAF-mutated mCRC. Between mCRC diagnosis and death or withdrawal, patients were frequently exposed to fluoropyrimidine (99.0%), irinotecan (96.2%), oxaliplatin (88.4%), anti-vascular endothelial growth factor (78.7%) and anti-epidermal growth factor receptor (40.1%). Median OS was 36.4, 7.1, and 6.6 months from mCRC diagnosis, inclusion into PROMETCO and third-line (3L) treatment initiation, respectively. Median PFS decreased significantly from first-line (9.2 months) to 3L (2.7 months) and remained consistent from 3L to sixth-line treatment (∼2.3 months). Median OS from diagnosis was 32.7, 26.8, and 40.6 months in RAS-mutated, BRAF-mutated, and RAS/BRAF wildtype mCRC patients, respectively.

Conclusions

PROMETCO provided information on real-world prescribing patterns and efficacy. OS from mCRC diagnosis and PFS from 3L and beyond were similar to previous long-term follow-up data from clinical trials.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信